Stereochemistry of the S N2? reaction in cyclohex-2-enyl esters
- 1 January 1977
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 20,p. 722-723
- https://doi.org/10.1039/c39770000722
Abstract
The SN2′ displacement of the cyclohex-2-enyl esters (1), (2), and (5) by piperidine proceeds with syn stereochemistry; the apparent anti products originate by SN2 reaction of the rearranged esters (15), (12), and (14).Keywords
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